Medical emergency?Emergency? Call 911. Nearest emergency roomsNearest ERs

Over-the-counter medicine · no prescription needed

Dextran 70 and hypromellose

Purpose on the label: Lubricant Lubricant

Eye care

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Dextran 70 and hypromellose used for?
The Drug Facts label of Walgreens Lubricant Eye Drops Preservative Free (Walgreen Company) lists these uses: temporary relief of discomfort due to dryness of the eye or to exposure to wind or sun.
Do I need a prescription for Dextran 70 and hypromellose?
No. The products on this page are sold without a prescription (over the counter).
Is a store brand the same as the name brand?
Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
Has Dextran 70 and hypromellose been recalled?
No recall linked to these products appears in the FDA enforcement reports we use.

Drug Facts label

Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.

Walgreens Lubricant Eye Drops Preservative Free · Walgreen Company

Dextran 70 0.1% · Hypromellose, unspecified 0.3%, liquid (ophthalmic)

Active ingredient

Dextran 70 0.1% Hypromellose 0.3%

Purpose

Lubricant Lubricant

Uses

temporary relief of discomfort due to dryness of the eye or to exposure to wind or sun

Warnings

For external use only

Do not use

if this solution changes color or becomes cloudy if you are sensative to any ingredient in this product

When using this product

to avoid contamination, do not touch tip of container to any surface do not reuse once opened, discard

Stop use and ask a doctor if

you feel eye pain changes in vision occur redness or irritation of the eye(s) gets worse or lasts more than 72 hours

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

put 1 or 2 drops in the affected eye(s) as needed

Other information

store at 15°-25°C (59°-77°F)

Inactive ingredients

boric acid, disodium edetate hydrate, potassium chloride, purified water, sodium borate, sodium chloride

Questions?

Call 1-888-527-4276

— FDA label of Walgreens Lubricant Eye Drops Preservative Free, Walgreen Company, effective December 20, 2023. See the official label on DailyMed →

CVS Gentle Tears · CVS Pharmacy, Inc.

Dextran 70 0.1% · Hypromellose, unspecified 0.3%, solution/ drops (ophthalmic)

Active ingredient

Dextran 70 0.1% Hypromellose 0.3%

Purpose

Lubricant Lubricant

Uses

temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun

Warnings

For external use only

Do not use

if this solution changes color or becomes cloudy if you are sensitive to any ingredient in this product

When using this product

to avoid contamination, do not touch tip of container to any surface do not reuse once opened, discard

Stop use and ask a doctor if

you feel eye pain changes in vision occur redness or irritation of the eye(s) gets worse or lasts more than 72 hours

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

put 1 or 2 drops in the affected eye(s) as needed

Other information

store at 15°-25°C (59°-77°F)

Inactive ingredients

boric acid, disodium edetate hydrate, potassium chloride, purified water, sodium borate, sodium chloride

— FDA label of CVS Gentle Tears, CVS Pharmacy, Inc., effective December 30, 2025. See the official label on DailyMed →

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

Same medicine, other brands

Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.

Dextran 70 0.1% · Hypromellose, unspecified 0.3% · liquid (ophthalmic) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Walgreens Lubricant Eye Drops Preservative Free Walgreen Company DailyMed
Dextran 70 0.1% · Hypromellose, unspecified 0.3% · solution/ drops (ophthalmic) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
CVS Gentle Tears CVS Pharmacy, Inc. DailyMed

Companies that sell this medicine

The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.

  • Walgreen Company1 product
  • CVS Pharmacy, Inc.1 product

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. FDA rule for the Drug Facts label (21 CFR 201.66)

Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.

Report an error → · Information for medicine makers